structure of Ethyl 2-bromothiazole-4-carboxylate

Ethyl 2-bromothiazole-4-carboxylate

CAS No.: 100367-77-9
M. Wt: 236.086
M. Fa: C6H6BrNO2S
InChI Key: CNHISCQPKKGDPO-UHFFFAOYSA-N
Appearance: Yellow Solid

Names and Identifiers of Ethyl 2-bromothiazole-4-carboxylate

CAS Number

100367-77-9

EC Number

640-217-3

MDL Number

MFCD03788564

IUPAC Name

ethyl 2-bromo-1,3-thiazole-4-carboxylate

InChI

InChI=1S/C6H6BrNO2S/c1-2-10-5(9)4-3-11-6(7)8-4/h3H,2H2,1H3

InChIKey

CNHISCQPKKGDPO-UHFFFAOYSA-N

Canonical SMILES

CCOC(=O)C1=CSC(=N1)Br

UNSPSC Code

12352100

Physical and chemical properties of Ethyl 2-bromothiazole-4-carboxylate

Acidity coefficient

-1.50±0.10(Predicted)

Boiling Point

277.6±13.0 °C at 760 mmHg

Density

1.7±0.1 g/cm3

Exact Mass

234.930252

Flash Point

121.7±19.8 °C

Index of Refraction

1.570

LogP

2.44

Melting Point

48-52ºC

Molecular Formula

C6H6BrNO2S

Molecular Weight

236.086

PSA

67.43000

Sensitivity

Moisture & Light Sensitive

Solubility

soluble in Methanol

Storage condition

Keep Cold

Vapour Pressure

0.0±0.6 mmHg at 25°C

Safety Information of Ethyl 2-bromothiazole-4-carboxylate

Pictograms

Signal Word

Warning

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

Applications of Ethyl 2-bromothiazole-4-carboxylate

Ethyl 2-bromothiazole-4-carboxylate finds applications in various fields:

  • Pharmaceutical Industry: It serves as an intermediate in the synthesis of bioactive compounds and pharmaceuticals.
  • Corrosion Inhibition: Its effectiveness as a corrosion inhibitor makes it valuable in materials science, particularly for protecting metals in acidic environments.
  • Organic Synthesis: It is used as a building block for synthesizing more complex organic molecules.

Interaction Studies of Ethyl 2-bromothiazole-4-carboxylate

Studies on ethyl 2-bromothiazole-4-carboxylate have primarily focused on its interaction with metals, particularly its role as a corrosion inhibitor. Research has demonstrated that it effectively reduces the corrosion rate of copper when exposed to acidic media, indicating its potential for use in protective coatings and materials.

Physical sample testing spectrum (NMR) of Ethyl 2-bromothiazole-4-carboxylate

Physical sample testing spectrum (NMR) of Ethyl 2-bromothiazole-4-carboxylate

Retrosynthesis analysis of Ethyl 2-bromothiazole-4-carboxylate

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  • Route#2

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  • Route#3

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